Associated Papers
Exploratory analysis of HLA SNPs associated with occult HBV infection: a multicenter case-control study in Chinese blood donors.
Zhou L et al.
Human Genetics, 2025
Accurate affinity models for SH2 domains from peptide binding assays and free-energy regression.
Gagoski D et al.
Protein Science : a Publication of the Protein Society, 2025
41088778 (PubMed )
Supplement: PRO-34-e70317-s008.xlsx › _S6_-_PTMVar_-_Lyn
Accurate sequence-to-affinity models for SH2 domains from multi-round peptide binding assays coupled with free-energy regression.
Gagoski D et al.
Biorxiv : the Preprint Server for Biology, 2025
39764007 (PubMed )
Supplement: media-1.xlsx › _S6_-_PTMVar_-_Lyn
Long-read single-cell sequencing reveals expressions of hypermutation clusters of isoforms in human liver cancer cells.
Liu S et al.
Elife, 2024
Long-read single-cell sequencing reveals expressions of hypermutation clusters of isoforms in human liver cancer cells.
Liu S et al.
Biorxiv : the Preprint Server for Biology, 2023
Targeted transcriptome analysis using synthetic long read sequencing uncovers isoform reprograming in the progression of colon cancer.
Liu S et al.
Communications Biology, 2021
33907296 (PubMed )
Supplement: 42003_2021_2024_MOESM12_ESM.xlsx › Supplementary_Data_9
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A2-A04Y-01A.domain
SNP-specific extraction of haplotype-resolved targeted genomic regions.
Dapprich J et al.
Nucleic Acids Research, 2008
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